High-temperature lubricants

ABSTRACT

A composition comprising 
     (a) one or more lubricants or hydraulic based on mineral oil or synthetic oils and 
     (b) 0.05 to 5% by weight, relative to the total weight of the lubricant composition or hydraulic oil composition, of a mixture of 
     (1) at least one compound of the formula I or II ##STR1##  in which Y, Z, R 1 , R 2 , R 3 , R 4 , R 5 , R 6  and R 7  as well as a are as defined in patent claim 1 and 
     (2) at least one compound of the formulae III or IV ##STR2##  in which X, X 1 , X 2 , R 11 , R 12 , m, n, n*, k, b and M are as defined in patent claim 1.

The present invention relates to lubricant or hydraulic oil compositions which contain, as additives, a mixture of an oil-soluble 5-ring heterocyclic compound, which may be benzo-fused, with a tautomeric 2-mercapto-1,3-hetero-atom-aza group and a phosphorus compound, and to the use of these mixtures as additives in lubricants or hydraulic oils

To improve the application properties, additives are usually added to mineral and synthetic lubricants. To improve the anti-wear properties, extreme-pressure additives and wear-reducing additives are added to the lubricants. These additives must meet the requirement of not having a corroding action on the metal components to be lubricated and having good heat resistance.

Various types of zinc dialkyl dithiophosphates (ZDTP) are used throughout the world as anti-wear additives.

The use of 5-ring heterocyclic compounds, which may be benzo-fused, with a tautomeric 2-mercapto-1,3-heteroatomaza group and, if appropriate, further nitrogen atoms in the ring system as lubricant additives is known. In general, however, these show only inadequate anti-wear properties, especially at higher temperatures.

Thus, aminobenzothiazole disulfides, for example, morpholinobenzothiazole disulfide, in combination with ZDTP are described as lubricant additives or motor fuel additives in DE-A No. 2,605,655.

In U.S. Pat. No. 3,966,623, the synergistic mixture of mercaptobenzothiazole amine salts with 2,5-dimercapto-1,3,4-thiadiazole disulfides as corrosion inhibitors in lubricating oils is described.

Moreover, EP-A No. 150,957 describes the use of mercaptozothiazole amine salt solutions in excess amine for improving the antioxidative and anticorrosive properties of power transmission fluids. In addition, rhodamine amine salts are known from U.S. Pat. No. 3,779,919 as additives for improving the load-bearing capacity of synthetic turbine oils.

It has now been found that mixtures of oil-soluble 5-ring heterocyclic compounds which have a tautomeric 2-mercapto-1,3-heteroatom-aza group and may be benzo-fused, or amine salts thereof, with various derivatives of phosphoric acid esters, thio-, dithio- or trithio-phosphoric acid esters or phosphorous acid esters have particularly good wear-reducing properties, especially at a higher temperature, coupled at the same time with a reduced P-content of the mixtures.

The present invention relates to a composition comprising

(a) one or more lubricants or hydraulic oils based on mineral oil or synthetic oils and

(b) 0.05 to 5% by weight, relative to the total weight of the lubricant composition or hydraulic oil composition, of a mixture of

(1) at least one compound of the formula I or II ##STR3## in which Y is --O--, --S--, --NH-- or --NR⁹ --, with R⁹ being C₁ -C₁₂ -alkyl, Z is --CR⁸ -- or --N-- and R¹ is hydrogen, C₁ -C₁₂ -alkyl, C₁ -C₄ -alkoxy, C₂ -C₂₄ -alkoxycarbonyl or nitro, R² is hydrogen or unsubstituted or OH-substituted C₁ -C₂₄ -alkyl, R³ is hydrogen, C₁ -C₂₄ -alkyl or C₂ -C₂₄ -alkenyl, R⁴ is C₁ -C₂₄ -alkyl or C₂ -C₂₄ -alkenyl, or R³ and R⁴ together are a --C(R¹⁰)═N-CH₂ -CH₂ - radical, with R¹⁰ being hydrogen, C₁ -C₁₇ -alkyl or C₂ -C₁₇ -alkenyl, and R⁵ is hydrogen, --SH or C₁ -C₂₂ -alkyl, R⁶ is hydrogen, R⁷ is hydrogen or R⁶ and R⁷ together are a direct bond, R⁸ is hydrogen or C₁ -C₂₂ -alkyl or phenyl, or R⁷ and R⁸ together are carbonyl and a has the value 0 or 1 to 2, and

(2) at least one compound of the formulae III or IV ##STR4## in which X, X¹ and X² independently of one another are oxygen or sulfur, R¹¹ and R¹² are identical or different and are each C₁ -C₁₂ -alkyl which may be interrupted by --O--, --S-- or --C(O)O--, unsubstituted or C₁ -C₁₂ -alkyl-substituted phenyl or naphthyl, unsubstituted or C₁ -C₄ -alkyl-substituted C₅ -C₁₂ -cycloalkyl or C₇ -C₁₃ -aralkyl, and n is the number 1, 2 or 3, n* is the number 1 or 2, m is the number 1 or 2, k is the number 1 or 2 and b is the number 0 or 1, and, in the case of n or n* being 2 or also n being 3, the radicals R¹¹ are identical or different or two radicals R¹¹ can, together with the two heteroatoms X¹ and the P atom to which they are linked, form a 5-membered or 6-membered ring, and in which M is a k-valent metal cation, a proton or a compound HN.sup.⊕R¹³ R¹⁴ R¹⁵, R¹³ being hydrogen or unsubstituted or OH-substituted C₁ -C₃₀ -alkyl, R¹⁴ being hydrogen or C₁ -C₃₀ -alkyl and R¹⁵ being C₁ -C₃₀ -alkyl or C₁₈ -alkenyl, or R¹⁴ and R¹⁵ together forming a -C(R¹⁶)=N--CH₂ -CH₂ -- radical and R¹⁶ being hydrogen, C₁ -C₁₇ -alkyl or C₂ -C₁₇ -alkenyl, with the proviso that, if m is 2 and k is 1, two different radicals M are possible.

C₁ -C₁₂ -Alkyl groups R¹, R⁹, R¹¹ and R¹² are straight-chain or branched alkyl radicals, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl, straight-chain or branched pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl and dodecyl.

C₁ -C₁₇ -Alkyl groups R¹⁰ and R¹⁶ are straight-chain or branched alkyl radicals, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl, straight-chain or branched pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl and heptadecyl.

C₁ -C₂₂ -Alkyl groups R⁵ and R⁸ are straight-chain or branched alkyl radicals, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl, straight-chain or branched pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, eicosyl, heneicosyl, and docosyl.

C₁ -C₂₄ -Alkyl groups R², R³ and R⁴ are straight-chain or branched alkyl radicals, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl, straight-chain or branched pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, eicosyl, heneicosyl, docosyl, tricosyl and tetracosyl.

C₁ -C₃₀ -Alkyl groups R¹³, R¹⁴ and R¹⁵ are straight-chain or branched alkyl radicals, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl, straight-chain or branched pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, eicosyl, heneicosyl, docosyl, tricosyl, tetracosyl, pentacosyl, hexacosyl, octacosyl and triacontyl.

Hydroxy-substituted alkyl groups R² and R¹³ are hydroxy mono- or -poly-substituted alkyl, the hydroxyl group being preferably terminal in the case of monosubstitution. This is in particular 2-hydroxyethyl.

In C₁ -C₁₂ -alkyl groups R¹¹ and R¹², which are interrupted by --O--, --S-- or --C(O)O --, the heteroatom or the C(O)O group can be in any possible position, and the C₁ -C₁₂ -alkyl radical can be interrupted once or several times, and the interruption can be due to both identical or different heteroatoms and C(O)O groups. One interruption is preferred.

C₂ -C₁₇ -Alkenyl groups R¹⁰ and R¹⁶ and C₂ -C₂₄ -alkenyl groups R³ and R⁴ are straight-chain or branched alkenyl radicals which contain one or more, but preferably one double bond, for example vinyl, allyl, n-butenyl, 1,3-butadienyl, i-pentenyl, pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl, tridecenyl, 2-nonyl-2-butenyl, tetradecenyl, pentadecenyl, hexadecenyl and 8-heptadecenyl. Furthermore, alkenyl R³ and R⁴ can also be, for example, 2-octadecenyl, oleyl, nonadecenyl, eicosenyl, heneicosenyl, docosenyl, tricosenyl and tetracosenyl. 8-Heptadecenyl and oleyl are preferred.

C₁ -C₄ -Alkoxy R¹ can be, for example, methoxy, ethoxy, isopropoxy or n-butoxy.

C₂ -C₂₄ -Alkoxycarbonyl R¹ contains 1 -24 carbon atoms in the alkyl moiety and can be, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl or 2-ethylhexyloxycarbonyl.

In C₁ -C₁₂ -alkyl-substituted phenyl or naphthyl R¹¹ and R¹², the phenyl or naphthyl radical can be monosubstituted or polysubstituted, but preferably monosubstituted to disubstituted; C₁ -C₁₂ -alkyl is, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl, straight-chain or branched nonyl or dodecyl.

C₅ -C₁₂ -Cycloalkyl R¹¹ and R¹² is, for example, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, cyclodecyl or cyclododecyl, and preferably cyclohexyl.

C₁ -C₄ -Alkyl-substituted C₅ -C₁₂ -cycloalkyl R¹¹ and R¹² can be monosubstituted or polysubstituted, but preferably monosubstituted; examples are methylcyclohexyl, trimethylcyclohexyl, butylcyclohexyl or propylcyclopentyl.

C₇ -C₁₃ -Aralkyl R¹¹ and R¹² is, for example, benzyl, 1- or 2-phenethyl, 3-phenylpropyl, α, α-dimethylbenzyl, 2-phenylisopropyl, 2-phenylhexyl, benzhydryl or naphthylmethyl, but preferably benzyl.

A k-valent metal cation M is, for example, Li.sup.⊕, Na.sup.⊕ or K.sup.⊕ in the case of k=1 and is Mg²⊕, Ca²⊕, Ba²⊕ or Zn²⊕ in the case of k=2. However, the preferred metal cation M is Zn²⊕.

Preferably, a has the value 0 or 1 to 1.25, and particularly preferably 0 or 1.2.

Those compositions are preferred in which, in the compounds of the formulae I or II, Y is oxygen or sulfur, but especially sulfur.

Those compositions are also preferred in which, in the compounds of the formula I, R¹ is hydrogen or C₁ -C₁₂ -alkyl, especially hydrogen or C₁ -C₄ -alkyl and very particularly R¹ is hydrogen.

Moreover, those compositions are preferred in which, in the compounds of the formula I, R¹ is hydrogen and Y is sulfur.

In addition, those compositions are of interest in which, in the compounds of the formula II, Z is --CR⁸ --.

Those compositions are also of interest in which, in the compounds of the formula II, R⁶ is a direct bond together with R⁷, or in which, in the compounds of the formula II, R⁵ is hydrogen or --SH, especially hydrogen.

Those compositions are also of interest in which, in the compounds of the formulae I or II, R² is hydrogen or unsubstituted or OH-substituted C₁ -C₄ -alkyl, especially hydrogen or methyl; and also those in which, in the compounds of the formulae I or II, R³ is hydrogen, C₈ -C₂₄ -alkyl or C₈ -C₂₄ -alkenyl; or in which, in the compounds of the formulae I or II, R⁴ is C₈ -C₂₄ -alkyl or C₈ -C₂₄ -alkenyl.

Those compositions are of particular interest in which, in the compounds of the formulae I or II, R² is hydrogen and R³ and R⁴ independently of one another are C₈ -C₂₄ -alkyl or C₈ -C₂₄ -alkenyl; and also those in which, in the compounds of the formulae I or II, R² and R³ are methyl and R⁴ is C₈ -C₂₄ -alkyl or C₈ -C₂₄ -alkenyl; or those in which, in the compounds of the formulae I or II, R² and R³ are hydrogen and R⁴ is C₈ -C₂₄ -alkyl or C₈ -C₂₄ -alkenyl.

C₈ -C₂₄ -Alkyl radicals R³ and R⁴ are preferably branched C₈ -C₂₄ -alkyl radicals, in particular those which contain tertiary C atoms, and particularly preferably those with a tertiary C atom in the α-position to the N atom, to which they are linked. In the case of, for example, a primary amine NR² R³ R⁴, those mixtures of such amines are preferably used which are commercially available under the description "Primene". Thus, for example, the mixture "Primene® 81-R" (mainly branched alkylamines having 12 to 15 C atoms) or the mixture "Primene® JM-T" (mainly branched alkylamines having 18 to 24 C atoms) can be used.

Those compositions are also of interest in which, in the compounds of the formulae I or II, R² is 2-hydroxyethyl and R³ together with R⁴ is a --C(R¹⁰)═N--CH₂ CH₂ -- radical, R¹⁰ being hydrogen, C₁ -C₁₇ -alkyl or C₂ -C₁₇ -alkenyl, but preferably C₈ -C₁₇ -alkyl or C₈ -C₁₇ -alkenyl.

A further embodiment is represented by compositions in which, in the compounds of the formulae III or IV, R¹¹ is C₁ -C₁₂ -alkyl which may be interrupted by --O--, --S-- or --C(O)O--, or phenyl or naphthyl which are unsubstituted or substituted by C₁ -C₁₂ -alkyl, especially C₈ -C₁₂ -alkyl, or cyclohexyl or benzyl, R¹¹ preferably being C₃ -C₁₂ -alkyl which may be interrupted by --C(O)O--, or phenyl or nonylphenyl.

An additional embodiment is represented by compositions in which, in the compounds of the formulae III or IV, R¹² is C₁ -C₁₂ -alkyl which may be interrupted by --O--, --S-- or --C(O)O --, or phenyl or naphthyl which are unsubstituted or substituted by C₁ -C₁₂ -alkyl, especially C₈ -C₁₂ -alkyl, or cyclohexyl or benzyl, R¹² preferably being C₃ -C₁₂ -alkyl which may be interrupted by --C(O)O --, or phenyl or nonylphenyl.

Those compositions are also of interest in which, in the compounds of the formulae III or IV, X is oxygen, and also those in which, in the compounds of the formulae III or IV, X¹ and X² are oxygen, or those in which, in the compounds of the formulae III or IV, X and X² are sulfur and X¹ is oxygen.

Moreover, those compounds are of interest in which, in the compounds of the formula III, M is a proton, Zn²⁺ or HN.sup.⊕ R¹³)(R¹⁴)(R¹⁵)

Those compositions are of particular interest in which, in the compounds of the formula III, X and X² are sulfur, X¹ is oxygen, R¹¹ is C₃ -C₈ -alkyl, n* is 2, m is 1 and M is Zn² +; or those in which, in the compounds of the formula III, X, X¹ and X² are oxygen, R¹¹ is C₂ -C₆ -alkyl, n* is 1 or 2, m is 2 or 1 and, in the case of m=1, M is HN.sup.⊕ R¹³)(R¹⁴)(R¹⁵) and, in the case of m=2, M is HN.sup.⊕ R¹³)(R¹⁴)(R¹⁵) or a proton, with the proviso that at most one radical M is a proton, R¹³ being preferably hydrogen and R¹⁴ and R¹⁵ independently of one another being C₈ -C₂₄ -alkyl.

Those compositions are of additional interest in which, in the compounds of the formulae III or IV, X is sulfur, and also those in which, in the compounds of the formulae III or IV, X is sulfur and X¹ and X² are oxygen; or those in which, in the compounds of the formulae III or IV, X is oxygen and X¹ and X² are sulfur.

Those compositions are also of interest in which, in the compounds of the formula III, R¹³ is 2-hydroxyethyl and R¹⁴ together with R¹⁵ is a --C(R¹⁶)═N--CH₂ -CH₂ -- radical, R¹⁶ preferably being C₈ -C₁₇ -alkyl or C₈ -C₁₇ -alkenyl.

Those compositions are preferred in which the mixture b) consists of (1) one compound of the formulae I or II and (2) one compound of the formula III.

Those compositions are particularly preferred in which, in the compounds of the formulae I or II, a has the value 0, Y is sulfur or oxygen, but preferably sulfur, and, in the formula I, R¹ is hydrogen and, in the compounds of the formula III, X, X¹ and X² are oxygen, R¹¹ is C₂ -C₆ -alkyl, n* is the number 1 or 2, m is the number 2 or 1 and, in the case of m=1, M is HN.sup.⊕ R¹³)(R¹⁴)(R¹⁵) and, in the case of m=2, M is HN.sup.⊕ (R¹³)(R¹⁴)(R¹⁵) or a proton, with the proviso that at most one radical M is a proton.

Those compositions are also preferred in which, in the compounds of the formulae I or II, a has the value 1 to 1.25, Y is sulfur or oxygen, but preferably sulfur, and, in the formula I, R¹ is hydrogen and, in the compounds of the formula III, X and X² are sulfur, X¹ is oxygen, R¹¹ is C₃ -C₈ -alkyl, n* is the number 2, m is the number 1 and M is Zn²⁺,

Those compositions are very particularly preferred in which the mixture (b) consists of (1) one compound of the formula I and (2) one compound of the formula III.

Those compositions are especially preferred in which, in the compounds of the formula I, a has the value 1 to 1.25, Y is sulfur, R¹ is hydrogen, R² is hydrogen, R³ is hydrogen or C₈ -C₂₄ -alkyl and R⁴ is C₈ -C₂₄ -alkyl and, in the compounds of the formula III, X and X² are sulfur, X¹ is oxygen, R¹¹ is C₃ -C₈ -alkyl, n* is the number 2, m is the number 1 and M is Zn²⁺.

The components of the mixtures (b), which can be used according to the invention, are known. The heterocyclic compounds are commercially available or can readily be prepared by generally known methods of organic chemistry from commercial products. Their amine salts are obtained in the conventional manner by addition of the corresponding amine (salt formation). An excess of the amine can also be used here (a>1). The preparation of the phosphorus compounds is described, for example, in Houben-Weyl "Methoden der organischen Chemie [Methods of organic chemistry]", volume 12, part 2, 4th edition, G. Thieme Verlag, Stuttgart 1964, on pages 53-77, 143-210, 226-274, 299-376 and 587-748. Their amine salts are prepared analogously to those of the heterocyclic compounds.

The mixtures (b) are prepared by methods known per se, for example by simple mixing. Thus, for example, 2-mercaptobenzothiazole can be incorporated into a commercially available amine phosphate (amine salts of monoesters/diesters of phorphoric acid).

The mixtures (b) are of a liquid nature, but have varying viscosities. They are outstandingly suitable as excellent anti-wear additives for lubricants and hydraulic oils, preferably for lubricants. The mixtures according to the invention deploy their full effectiveness especially at high temperatures.

The present invention therefore also relates to the use of mixtures of (1) at least one compound of the formulae I or II and (2) at least one compound of the formulae III or IV as wear-reducing additives for lubricants or hydraulic oils.

The mixtures (b) are soluble in lubricants and hydraulic oils in an adequate quantity and are employed in a concentration from 0.05 to 5% by weight, preferably in a concentration from 0.1 to 3% by weight, relative to the total weight of the lubricant composition or hydraulic oil composition.

The (1):(2) ratio is, for example, 10:1 to 1:10, preferably 5:1 to 1:10 and particularly preferably 2:1 to 1:5, especially 1:1 to 1:3.

The mixtures can be added as such to the lubricant, or the components, for example 2-mercaptobenzothiazole amine salts and the phosphorus compound, can be prepared separately and added to the lubricant separately during formulation. In the case of highly viscous mixtures, dilution with, for example, an appropriate base oil represents an advantageous form for making up.

The lubricants or hydraulic oils in question are familiar to those skilled in the art and are described, for example, in the "Schmiermittel Taschenbuch [Lubricants Handbook]" (Huthig Verlag, Heidelberg, 1974), or in "Ullmanns Encyclopadie der technischen Chemie [Ullmann's Encyclopedia of Industrial Chemistry]", volume 13, pages 85-94 (Verlag Chemie, Weinheim, 1977).

Particularly suitable examples, apart from mineral oils, are poly-α-olefins, ester-based lubricants, phosphate esters, glycols, polyglycols and polyalkylene glycols.

Moreover, the lubricants can contain other additives added for even further improvement of the basic properties of lubricants and hydraulic oils; these include antioxidants, metal passivators, rust inhibitors, viscosity index improvers, pour point depressants, dispersants, detergents, extreme-pressure additives and other anti-wear additives.

Examples of phenolic antioxidants

1. Alkylated monophenols

2,6-di-tert-Butyl-4-methylphenol, 2,6-di-tert-butyl-phenol, 2-tert-butyl-4,6-dimethylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butyl-4-n-butylphenol, 2,6-di-tert-butyl-4-isobutylphenol, 2,6-di-cyclopentyl-4-methylphenol, 2-(α-methylcyclohexyl)-4,6-dimethylphenol, 2,6-di-octadecyl-4-methylphenol, 2,4,6-tri-cyclohexylphenol, 2,6-di-tert-butyl-4-methoxymethylphenol and o-tert-butylphenol.

2. Alkylated hydroquinones

2,6-di-tert-Butyl-4-methoxyphenol, 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amyl-hydroquinone and 2,6-diphenyl-4-octadecyloxyphenol.

3. Hydroxylated thiodiphenyl ethers

2,2'-Thio-bis-(6-tert-butyl-4-methylphenol), 2,2'-thio-bis-(4-octylphenol), 4,4'-thio-bis-(6-tert-butyl-3-methylphenol) and 4,4'-thio-bis-(6-tert-butyl-2-methylphenol).

4. Alkylidene-bisphenols

2,2'-Methylene-bis-(6-tert-butyl-4-methylphenol), 2,2'-methylene-bis-(6-tert-butyl-4-ethylphenol), 2,2'-methy-lene-bis-[4-methyl-6-(α-methylcyclohexyl)-phenol], 2,2'- methylene-bis-(4-methyl-6-cyclohexylphenol), 2,2'-methylene-bis-(6-nonyl-4-methylphenol), 2,2'-methylene-bis-(4,6-di-tert-butylphenol), 2,2'-ethylidene-bis-(4,6-di-tert-butylphenol), 2,2'-ethylidene-bis-(6-tert-butyl-4-iso-butylphenol), 2,2'-methylene-bis-[6-(α-methylbenzyl)-4-nonylphenol], 2,2'-methylene-bis-[6-(α,α-dimethylbenzyl)-4-nonylphenol], 4,4'-methylene-bis-(2,6-di-tert-butylphenol), 4,4'-methylene-bis-(6-tert-butyl-2-methylphenol), 1,1-bis-(5-tert-butyl-4-hydroxy-2-methylphenyl)-butane, 2,6-di-(3-tert-butyl-5-methyl-2-hydroxybenzyl)-4-methylphenol, 1,1,3-tris-(5-tert-butyl-4-hydroxy-2-methylphenyl)-3-n-dodecyl-mercaptobutane, ethylene glycol bis-[3,3-bis-(3'-tert-butyl-4'-hydroxyphenyl)-butyrate], di-(3-tert-butyl-4-hydroxy-5-methylphenyl)-dicyclopentadiene, di-[2-(3'-tert-butyl-2'-hydroxy-5'-methyl-benzyl)-6-tert-butyl-4-methyl-phenyl]terephthalate.

5. Benzyl compounds

1,3,5-Tri-(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene, di-(3,5-di-tert-butyl-4-hydroxybenzyl) sulfide, isooctyl 3,5-di-tert-butyl-4-hydroxybenzyl-mercapto acetate, bis-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl) dithiol terephthalate, 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate, 1,3,5-tris-(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl) isocyanurate, dioctadecyl 3,5-di-tert-butyl-4-hydroxybenzyl-phosphonate and the calcium salt of monoethyl 3,5-di-tert-butyl-4-hydroxybenzyl-phosphonate.

6. Acylaminophenols

Lauric acid 4-hydroxyanilide, stearic acid 4-hydroxyanilide, 2,4-bis-octylmercapto-6-(3,5-di-tert-butyl-4-hyd-roxyanilino)-s-triazine and octyl N-(3,5-di-tert-butyl-4-hydroxyphenyl)-carbamate.

7. Esters of β-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid with monohydric or polyhydric alcohols, for example with methanol, octadecanol, 1,6-hexanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris-hydroxyethyl isocyanurate and di-hydroxyethyl-oxamide.

8. Esters of β-(5-tert-butyl-4-hydroxy-3-methylphenyl)propionic acid with monohydric or polyhydric alcohols, for example with methanol, octadecanol, 1,6-hexanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris-hydroxyethyl isocyanurate and di-hyd- roxyethyl-oxamide.

9. Amides of β-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid, for example N,N'-di-(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)-hexamethylenediamine, N,N'-di-(3,5-di-tert-butyl-4-hydroxyphenyl-propionyl)-trimethylenediamine and N,N'-di-(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)-hydrazine.

Examples of amine-type antioxidants

N,N'-Di-isopropyl-p-phenylenediamine, N,N'-di-secbutyl-p-phenylenediamine, N,N'-bis(1,4-dimethyl-pentyl)-p-phenylenediamine, N,N'-bis(1-ethyl-3-methyl-pentyl)-p-phenylenediamine, N,N'-bis(1-methyl-heptyl)-p-phenylenediamine, N,N'-diphenyl-p-phenylenediamine, N,N'-di-(naphthyl-2)-p-phenylenediamine, N-isopropyl-N'-phenyl-p-phenylenediamine, N-(1,3-dimethyl-butyl)-N'-phenyl-p-phenylenediamine, N-(1-methyl-heptyl)-N'-phenyl-p-phenylenediamine, N-cyclohexyl-N'-phenyl-p-phenylenediamine, 4-(p-toluene-sulfonamido)-diphenylamine, N,N'-dimethyl-N,N'-di-sec-butyl-p-phenylenediamine, diphenylamine, 4-isopropoxy-diphenylamine, N-phenyl-1-naphthylamine, N-phenyl-2-naphthylamine, octylated diphenylamine, 4-n-butylaminophenol, 4-butyrylamino-phenol, 4-nonanoylaminophenol, 4-dodecanoylamino-phenol, 4-octadecanoylamino-phenol, di-(4-methoxy-phenyl)-amine, 2,6-di-tert-butyl-4-dimethyl- amino-methyl-phenol, 2,4'-diamino-diphenylmethane, 4,4'-diamino-diphenylmethane, N,N,N',N'-tetramethyl-4,4'-diaminodiphenylmethane, 1,2-di-[(2-methyl-phenyl)-amino]-ethane, 1,2-di-(phenylamino)-propane, (o-tolyl)-biguanide, di-[4-(1',3'-dimethyl-butyl)-phenyl)-amine, tert-octylated N-phenyl-1-naphthylamine and a mixture of monoalkylated and dialkylated tert-butyl/tert-octyldiphenylamines.

Examples of metal passivators are

for copper, for example triazole, benzotriazole and derivatives of these, salicylidene-propylenediamine and salts of salicylaminoguanidine.

Examples of rust inhibitors are

(a) organic acids, their esters, metal salts and anhydrides, for example: N-oleoyl-sarcosine, sorbitan monooleate, lead naphthenate, dodecenylsuccinic anhydride, alkenylsuccinic acid half esters and 4-nonylphenoxyacetic acid.

(b) Nitrogenous compounds, for example:

I. Primary, secondary or tertiary aliphatic or cycloaliphatic amines and amine salts of organic and inorganic acids, for example oil-soluble alkylammonium carboxylates.

II. Heterocyclic compounds, for example: substituted imidazolines and oxazolines.

(c) Phosphorus-containing compounds, for example: amine salts of phosphoric acid partial esters.

(d) Sulfur-containing compounds, for example: barium dinonylnaphthalenesulfonates and calcium petroleum-sulfonates.

Examples of viscosity index improvers are

polymethacrylates, vinylpyrrolidone/methacrylate copolymers, polybutenes, olefin copolymers and styrene/acrylate copolymers.

Examples of pour point depressants are

polymethacrylate and alkylated naphthalene derivatives.

Examples of dispersants/surfactants are

polybutenylsuccinmides, polybutenylphosphonic acid derivatives and basic magnesium, calcium and barium sulfonates and phenolates.

Examples of anti-wear additives are

compounds containing sulfur and/or phosphorus and/or halogen, such as sulfurated vegetable oils, zinc dialkyl dithiophosphates, tritolyl phosphate, chlorinated paraffins, alkyl disulfides and aryl disulfides.

In the examples which follow, parts and percentages relate to the weight, unless otherwise stated.

EXAMPLES 1-9

The amine salts shown in Table 1 which follows are obtained by combining appropriate molar proportions of the heterocyclic mercapto compound with an amine.

                                      TABLE 1                                      __________________________________________________________________________          Heterocyclic                        SH compound/                                                                           Physical                           mercapto                            amine molar                                                                            data                          Example                                                                             compound    Amine                   ratio   M.p./n.sub.D.sup.20           __________________________________________________________________________           ##STR5##   H.sub.2 N-tert.-C.sub.12 /.sub.14 H.sub.25 /.sub.29.sup.(                      1)                      1:1.2   dark viscous liquid           2                                                                                    ##STR6##                                                                                   ##STR7##               1:1.2   M.p. 52-55° C.         3                                                                                    ##STR8##   H.sub.2 N-tert.-C.sub.12 /.sub.14 H.sub.25 /.sub.29.sup.(                      1)                      1:1.2   1.5713                        4                                                                                    ##STR9##   H.sub.2 N-tert.-C.sub.18 /.sub.22 H.sub.37 /.sub.45.sup.(                      2)                      1:1.2   1.5379                        5                                                                                    ##STR10##  H.sub.2 NC.sub.18 H.sub.35                                                                             1:1.2   M.p. 47-52° C.         6                                                                                    ##STR11##  H.sub.2 N-tert.-C.sub.12 /.sub.14 H.sub.25 /.sub.29.sup.(                      1)                      1:1.2   1.5440                        7                                                                                    ##STR12##  H.sub.2 N-tert.-C.sub.18 /.sub.24 H.sub.37 /.sub.45.sup.(                      2)                      1:1.2   1.5543                        8                                                                                    ##STR13##                                                                                  ##STR14##              1:1.2   1.5569                        9                                                                                    ##STR15##  HN[C.sub.13 H.sub.27 ].sub.2                                                                           1:1.2   1.5297                        __________________________________________________________________________      .sup.(1) Primene ®81-R (Rohm and Haas)                                     .sup.(2) Primene ®JM-T (Rohm and Haas)                               

EXAMPLES 10-14

The mixtures shown in Table 2 are obtained analogously to Examples 1-9 by adding an appropriate phosphorus compound to a heterocyclic mercapto compound.

                                      TABLE 2                                      __________________________________________________________________________          Heterocyclic                 Mixing                                       Example                                                                             mercapto compound                                                                        P compounds        ratio                                                                              n.sub.D.sup.20                           __________________________________________________________________________     10   2-Mercaptobenzo-                                                                         Monohexyl/dihexyl phosphate/                                                                      1:3 1.5240                                        thiazole  tetramethylnonylamines.sup.3                                    11   2,5-Dimercapto-                                                                          Dioctyl phosphite  1:9 1.4645                                        1,3,4-thiadiazole                                                         12   2-Mercapto-4-                                                                            O,O-Diisopropyl S-carbohexoxymethyl                                                               1:9 1.4790                                        methyl-1,3-thiazole                                                                      thiophosphate                                                   13   3-Mercaptobenzo-                                                                         Monononyl-/dinonyl-phenyl phosphite/                                                              15:85                                                                              1.5362                                        thiazole  N-di-2-ethylhexylamine                                          14   3-Mercapto-4-                                                                            Dibutyl phosphite  1:9 1.4415                                        methyl-1,2,4-                                                                  triazole                                                                  __________________________________________________________________________      .sup.3 CAS-Registry No. 8093962-4                                        

EXAMPLES 15-24

The mixtures shown in Table 3 are prepared by adding compounds from Table 1 to phosphorus compounds.

                                      TABLE 3                                      __________________________________________________________________________          Product accord-                     Mixing                                Example                                                                             ing to Example                                                                         P compounds        Further additives                                                                       ratio                                                                              n.sub.D.sup.20                    __________________________________________________________________________     15   3       O,O-Diisopropyl S-2-carboethoxyethyl                                                              --       1:1 1.5318                                         dithiophosphate                                                   16   9       Monohexyl/dihexyl phosphate/tetra-                                                                --       1:1 1.4952                                         methylnonylamines.sup.3                                           17   4       Zinc dialkyl dithiophosphate (ZDTP)                                                               Antioxidant.sup.4                                                                       2:3:2                                                                              1.5404                            18   4       S,S,S-Tris-carbo-2-ethylhexoxymethyl                                                              Antioxidant.sup.4                                                                       2:1:1                                                                              1.5366                                         trithiophosphate                                                  19   4       S,S,S-Tris-carbo-2-ethylhexoxymethyl                                                              Antioxidant.sup.4                                                                       1:1:1                                                                              1.5357                                         trithiophosphate                                                  20   8       Dioctyl phosphite  --       1:1 1.4992                            21   5       Dioctyl phosphite  --       1:1 1.5044                            22   9       Triphenyl thionophosphate                                                                         --       1:1                                   23   3       Monohexyl/dihexyl phosphate/tetra-                                                                --       1:1                                                methylnonylamines.sup.3                                           24   3       Zinc dialkyl dithiophosphate (ZDTP)                                                               --       1:1.5                                 __________________________________________________________________________      .sup.3 CAS-Registry No. 8093962-4                                              .sup.4 Mixture of monoalkylated and dialkylated tert. butyl/tert.              octyldiphenylamines.                                                     

EXAMPLE 25

The mixtures (b) are tested under various loadings in a shell 4-ball tester in a paraffinic base oil according to DIN 51,350 part 3. The wear scar diameter WSD is taken as a measure of the wear.

    ______________________________________                                                           Conc.            Time  WSD                                   Test  Example No. [%]      Loading [min] [mm]                                  ______________________________________                                         1     16          1        1000    5     0.71                                  2     16          1        1300    10    0.47                                  3     22          1        1300    5     1.9                                   4     22          1         800    5     0.83                                  ______________________________________                                    

EXAMPLE 26

The anti-wear effect is determined by means of a commercial oscillating friction apparatus from Optimol GmbH, Munich. (R. Schumacher et al. ASLE Transaction 26, 1 (1983), 94-101).

This apparatus is based on the following principle: a steel ball (100 Cr 6) subject to a force F_(N) oscillates on a steel cylinder. The ball is fixed in a holder and accordingly executes an oscillating sliding motion. The horizontal and vertical forces are determined by a piezoelectric force sensor. Under the present test conditions, the maximum Herz normal stress is 2740 N/mm² and the maximum shear stress is 850 N/mm². The ball and the cylinder have been made of the same tool steel.

A few drops of oil, which contains the compound to be tested in solution, are applied between the cylinder and the ball. The following test conditions are chosen: Loading: 200 N, frequency: 50 Hz, amplitude: 1000 μ, temperature: 130°-150° C., test period: 2 hours. Test oil: ISO VG 100 polyalphaolefin, S content <1.5 ppm.

To characterize the wear, a transverse profile is taken by means of a stylus instrument (Talysurf from Rank Taylor Hobson, Leicester, England). The integrated transverse profile area is taken as a measure of wear. The values given represent a relative measure of wear. The true wear value is calculated by multiplication with the factor F=2×10⁴.

    ______________________________________                                                 Concentration Wear: mm.sup.2                                           Additive  [%]             130° C.                                                                         150° C.                               ______________________________________                                         Example 22                                                                               2               8.9     24.8                                         ______________________________________                                    

EXAMPLE 27

Procedure as in Example 26. Test temperatures 100° C., 120° C., 150° C.

    ______________________________________                                                Concentration                                                                             Wear: mm.sup.2                                               Additive [%]          100° C.                                                                          130° C.                                                                        150° C.                           ______________________________________                                         Example 23                                                                              2            4.4      2.2    3.3                                      ______________________________________                                    

EXAMPLE 28

Procedure as in Example 26. Test temperatures 130° C.-150° C. Test oil I: Paraffin-type base oil ISO VG 32 with commercially available additives

0.75% of zinc dialkyl dithiophosphate (ZDTP)

11% of detergent

6% of viscosity index improver

Test oil II: Test oil I +0.5% of Example 3.

Test oil II thus contains Example 24 as the mixture b).

    ______________________________________                                         Temperature     Wear: mm.sup.2                                                 [°C.]    Test oil I                                                                              Test oil II                                           ______________________________________                                         130             11.1     1.4                                                   140             19.3     2.8                                                   150             >25.0    4.5                                                   ______________________________________                                     

What is claimed is:
 1. A composition consisting essentially of(a) one or more lubricants or hydraulic oils based on mineral oil or synthetic oils and (b) 0.05 to 5% by weight, relative to the total weight of the lubricant composition or hydraulic oil composition, of a mixture of(1) at least one compound of the formula I or II ##STR16## in which Y is --O--, --S--, --NH-- or --NR⁹ --, with R⁹ being C₁ -C₁₂ -alkyl, Z is --CR⁸ -- or --N-- and R¹ is hydrogen, C₁ -C₁₂ -alkyl, C₁ -C₄ -alkoxy, C₂ -C₂₄ -alkoxycarbonyl or nitro, R² is hydrogen or unsubstituted or OH-substituted C₁ -C₂₄ -alkyl, R³ is hydrogen, C₁ -C₂₄ -alkyl or C₂ -C₂₄ -alkenyl, R⁴ is C₁ -C₂₄ -alkyl or C₂ -C₂₄ -alkenyl, or R³ and R⁴ together are a --C(R¹⁰)═N--CH₂ -CH₂ - radical, with R¹⁰ being hydrogen, C₁ -C₁₇ -alkyl or C₂ -C₁₇ -alkenyl, and R⁵ is hydrogen, --SH or C₁ -C₂₂ -alkyl, R⁶ is hydrogen, R⁷ is hydrogen or R⁶ and R⁷ together are a direct bond, R⁸ is hydrogen or C₁ -C₂₂ -alkyl or phenyl, or R⁷ and R⁸ together are carbonyl and a has the value 0 or 1 to 2, and (2) at least one compound of the formulae III or IV ##STR17## in which X, X¹ and X² independently of one another are oxygen or sulfur, R¹¹ and R¹² are identical or different and are each C₁ -C₁₂ -alkyl which may be interrupted by --O--, --S-- or --C(O)O --, unsubstituted or C₁ -C₁₂ -alkyl-substituted phenyl or naphthyl, unsubstituted or C₁ -C₄ -alkyl-substituted C₅ -C₁₂ -cycloalkyl or C₇ -C₁₃ -aralkyl, and n is the number 1, 2 or 3, n* is the number 1 or 2, m is the number 1 or 2, k is the number 1 or 2 and b is the number 0 or 1, and, in the case of n or n* being 2 or also n being 3, the radicals R¹¹ are identical or different or two radicals R¹¹ can, together with the two heteroatoms X¹ and the P atom to which they are linked, form a 5-membered or 6-membered ring, and in which M is a k-valent metal cation, a proton or a compound HN⁺ R¹³ R¹⁴ R¹⁵, R¹³ being hydrogen or unsubstituted or OH-substituted C₁ -C₃₀ -alkyl, R¹⁴ being hydrogen or C₁ -C₃₀ -alkyl and R¹⁵ being C₁ -C₃₀ -alkyl or C₁₈ -alkenyl, or R¹⁴ and R¹⁵ together forming a -C(R¹⁶)═N--CH₂ -CH₂ -- radical and R¹⁶ being hydrogen, C₁ -C₁₇ -alkyl or C₂ -C₁₇ -alkenyl, with the proviso that, if m is 2 and k is 1, two different radicals M are possible.
 2. A composition according to claim 1, wherein, in the formula I, R¹ is hydrogen and Y is --S--.
 3. A composition according to claim 1, wherein, in the formula II, R⁶ together with R⁷ is a direct bond.
 4. A composition according to claim 1, wherein, in the formulae I or II, R² is hydrogen or unsubstituted or OH-substituted C₁ -C₄ -alkyl.
 5. A composition according to claim 1, wherein, in the formulae I or II, R² is hydrogen and R³ and R⁴ independently of one another are each C₈ -C₂₄ -alkyl or C₈ -C₂₄ -alkenyl.
 6. A composition according to claim 1, wherein, in the formulae I or II, R² and R³ are hydrogen and R⁴ is C₈ -C₂₄ -alkyl or C₈ -C₂₄ -alkenyl.
 7. A composition according to claim 1, wherein, in the formulae I or II, R² is 2-hydroxyethyl and R³ together with R⁴ is a -C(R¹⁰)═N--CH₂ -CH₂ -- radical.
 8. A composition according to claim 1, wherein, in the formulae III or IV, R¹¹ is C₁ -C₁₂ -alkyl which may be interrupted by --O--, --S-- or --C(O)O, or unsubstituted or C₁ -C₁₂ -alkyl-substituted phenyl or naphthyl, or cyclohexyl or benzyl.
 9. A composition according to claim 1, wherein, in the formulae III or IV, R¹² is C₁ -C₁₂ -alkyl which may be interrupted by --O--, --S-- or --C(O)O--, or unsubstituted or C₁ -C₁₂ -alkyl-substituted phenyl or naphthyl, or cyclohexyl or benzyl.
 10. A composition according to claim 1, wherein, in the formula III, M is a proton, Zn²⁺ or HN.sup.⊕(R¹³)(R¹⁴)(R¹⁵)
 11. A composition according to claim 1, wherein, in the formula III, X and X² are sulfur, X¹ is oxygen, R¹¹ is C₃ -C₈ -alkyl, n* is 2, m is 1 and M is Zn²⁺
 12. A composition according to claim 1, wherein, in the formula III, X, X¹ and X² are oxygen, R¹¹ is C₂ -C₆ -alkyl, n* is 1 or 2, m is 2 or 1 and M, in the case of m=1, is HN.sup.⊕ (R¹³)(R¹⁴)(R¹⁵) and, in the case of m=2, is HN.sup.⊕ (R¹⁴) (R¹⁵) or a proton, with the proviso that at most one radical M is a proton.
 13. A composition according to claim 1, wherein the mixture (b) consists of (1) one compound of the formulae I or II and (2) one compound of the formula III.
 14. A composition according to claim 13, wherein, in the compounds of the formulae I or II, a has the value 0, Y is sulfur or oxygen and, in the formula I, R¹ is hydrogen and, in the compounds of the formula III, X, X¹ and X² are oxygen, R¹¹ is C₂ -C₆ -alkyl, n* is the number 1 or 2, m is the number 2 or 1 and M, in the case of m=1, is HN.sup.⊕(R¹³)(R¹⁴)(R¹⁵) and, in the case of m=2, is HN.sup.⊕(R¹³)(R¹⁴)(R¹⁵), or a proton with the proviso that at most one radical M is a proton.
 15. A composition according to claim 13, wherein, in the compounds of the formulae I or II, a has the value 1 to 1.25, Y is sulfur or oxygen and, in the formula I, R¹ is hydrogen, and, in the compounds of the formula III, X and X² are sulfur, X¹ is oxygen, R¹¹ is C₃ -C₈ -alkyl, n* is the number 2, m is the number 1 and M is Zn²⁺.
 16. A composition according to claim 1, wherein the mixture (b) consists of (1) one compound of the formula I and (2) one compound of the formula III.
 17. A composition according to claim 16, wherein, in the compounds of the formula I, a has the value 1 to 1.25, Y is sulfur, R¹ is hydrogen, R² is hydrogen, R³ is hydrogen or C₈ -C₂₄ -alkyl and R⁴ is C₈ -C₂₄ -alkyl and, in the compounds of the formula III, X and X² are sulfur, X¹ is oxygen, R¹¹ is C₃ -C₈ -alkyl, n* is the number 2, m is the number 1 and M is Zn²⁺.
 18. Process of inhibiting the wear of lubricants or hydraulic oils which consists essentially of incorporating 1) at least one compound of the formulae I or II and 2) at least one compound of the formulae III or IV, according to claim 1, as wear-reducing additives to lubricants or hydraulic oils. 